CA2072869A1 - Dual lumen cannula - Google Patents
Dual lumen cannulaInfo
- Publication number
- CA2072869A1 CA2072869A1 CA002072869A CA2072869A CA2072869A1 CA 2072869 A1 CA2072869 A1 CA 2072869A1 CA 002072869 A CA002072869 A CA 002072869A CA 2072869 A CA2072869 A CA 2072869A CA 2072869 A1 CA2072869 A1 CA 2072869A1
- Authority
- CA
- Canada
- Prior art keywords
- body member
- cannula
- cross
- nipples
- bore
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
- A61M16/06—Respiratory or anaesthetic masks
- A61M16/0666—Nasal cannulas or tubing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
- A61M16/08—Bellows; Connecting tubes ; Water traps; Patient circuits
- A61M16/0816—Joints or connectors
- A61M16/0841—Joints or connectors for sampling
- A61M16/085—Gas sampling
Abstract
Inventor's Name: William Cartar Atty's. Docket No.: PB-8PCT
Dual Lumen Cannula ABSTRACT OF THE DISCLOSURE:
Cannula apparatus for respiration therapy, having a pair of body members, each having a pair of cannulae for providing a cannula nipple outlet for each of a person's nostrils, the two body members respectively delivering gas to each of the person's nostrils, and monitoring the respiration of each of the person's nostrils, One or the body members is carried inwardly of the other, its cannulae also carried inwardly of those of the other, achieving the patient comfort of only feeling a single cannula in each nostril, yet the gas and monitoring lumens and their outlets are separate for good operativity of respiration and breathing-monitoring.
Interchangeability of the body members and their respective tubing is provided by operative equality of areas of the cylindrical and annular passages.
Dual Lumen Cannula ABSTRACT OF THE DISCLOSURE:
Cannula apparatus for respiration therapy, having a pair of body members, each having a pair of cannulae for providing a cannula nipple outlet for each of a person's nostrils, the two body members respectively delivering gas to each of the person's nostrils, and monitoring the respiration of each of the person's nostrils, One or the body members is carried inwardly of the other, its cannulae also carried inwardly of those of the other, achieving the patient comfort of only feeling a single cannula in each nostril, yet the gas and monitoring lumens and their outlets are separate for good operativity of respiration and breathing-monitoring.
Interchangeability of the body members and their respective tubing is provided by operative equality of areas of the cylindrical and annular passages.
Description
2~28~9 Inventor'a Name: William C~rter Atty'o. Docket No.: PB-8PCT
Dual ~umen Cannula I. Field of the Invention-.
This invention relatea to respiration therapy, and more particularly to re~piration therapy in which a gas (usually oxygen or an oxygen/alr mixture) i~ to be dellvered into a patient's noatril~ by ~ome aort of a cannula inaerted into the patient'a no~e, and a breathlng-monitoring cannula le ~lao needed in close proximity to control details of the ov~rall reapiration-therapy equipment and procedure.
Such detalls, i.e., of breathing-monitoring, control of preaaure and ~upply of the resplration gas, sequential setting of the respiratlon equipment components, etc., are not part of this invention, but they are mentioned to indlcate th0 reason for the breathing~monitoring functibn to be needed;
and ~ince that breathing-monitoring fu~ction i~ needed, that is the reason why breathing-monitoring cannulae are needed in the patient~a nose even though the preaence of an e~tra cannula in each noatril is a aource of extra bother and discomfort to the patient, who is likely to find any sort of respiration therapy disagreeable to aay the lea~t.
2~7~8~
With auch reepiratlon therapy, therefOre~ the presence of two cannulae has long been known to be needed~ ln a dual arrangement providing a pair of cannulae and thelr gaa-delivery or monitoring bores (lumena) ln a eort of harne~a, with one tube going to the oxygen or air/oxygen supply, and one tube connected to either some monltor/control equipment or to another ga~.
Again~t that background, the present invention's achlevements are to provide better patient comfort, ease ~d convenience for the attendant, good operativlty, etc.
II. ~ummary of the Invention:
In carrying out the lnvention, there are provided a pair of body members, one being an inner one and one being an outer one, each havlng a primary bore and a apaced pair of cannula nipplea.
One of the oannula nipplee oE the outer body member, and one of the cannula nlpplee of the inner bod~ member, reapectively, are provided as a ~et, for each of a per~onls noetril~; and each set provides for one of the body members 2~2~9 a respiratlon gas and either a monitorlng of that gas or a supply of a dlfferent gas.
~ he cannula nipplea o~ the inner body member are made to be sui'ficlently fle~ible, preferably by the inner body memb~r being formed integrally with its cannula nipples~
all from a fle~ible material, that aasembly i~ aohleved by pushing the lnner body lnto an open end of the outer body;
and thie flexibllity accommodates assembly even though the nipplea of both body members extend transver~ely of the portlon of the Oody me~ber haYing its primary bore.
Interchangeability of either the inner body member and outer body member provldes for convenience of use; and thia lnterchangeabllity is achieved by providing all corresponding portlona of the inner and outer body ~ember~ o~ operatively equal cross-~ectlonal bore areas, i.e., the croaa-aectional area of the inner body memb~r is operatively equal to the cross-sectlonal area of the outer body member minu~ the cross-sectional area of the outer surface o~ the inner body member.
2072~6~
III. The prior art doe~ not show the inventive concepts, even though patlen~-theraEy~h~ long ~lIized--modi~led re~PlratlOn uein~ cannulae:
The prior art therapy has long provided var$ous modifications of human respiration, particularly oxygen and or ox~gen/air mlxtures; and, since it has been long known that the supply and rate of oxygen delivery to the patient must be kept within prescrlbed limita, and since ~upply-control equipment ha~ been provided which sen~es re~piration a~ a mean~ of economi~ing the oxygen delivery, the prior art ha~ provided not only an oxygen-supply tube arrangement but also a re~piration-monltoring tube to control the oxygen supply.
And sinoe humans have two no~trils, and since the re~piration o~ the two noatrils is often slgnificantly different, the prior art has provlded both an oxygen-supply tube and a breath-monitoring tube for each nos-tril.
Yet not only is oxygen therapy itself bothersome and annoying to many patient~ the e~tra monitoring tube u~e, 2~2869 making two tubes for each nostril, all accumulate to make oxygen therapy of additional di6comfort to the patient, especially of cour~e with the other discomforts of the therapy environment and ~ituation, The prlor art has provided monitoring equipment for monitoring the respiration cycle of a patient (inhaling, dwell, and exhaling periods) 80 aa to cause the oxygen or oxygen~air to be forced to the patient only at certain periods of the cycle (for both patient-comfort and oxygen economy);
and that monitoring has been provided by tubing whose open or ~en~ing end i~ in close proximity to the oxygen or oxygen/alr outlet.
It has apparently seemed inevitable to the prior art~
or at least an inherent lncident of oxygen 3upply and breath-monltoring,that ~eparate tube~ be pro~ided for the oxygen-3upply and for the breath-monitoring operativity for each nostril, and that each of the set for each nostril be kept eeparate to avoid undue masking of the resplration by the oxygen supply.
2~7~9 With thls background, the ~ignificance of the pre~ent invention, by which the patlent la required to be bothered by only a ~ingle cannula nlpple in each noetril, i8 better eeen to be quite advantageous, making tha oxygen therapy le~
bothersome and more endurable.
In a hindsight consideration ofthe present invention to determine its inventive and novel nature, it is not only conceded but emphasized that the prior art had details usable in this invention but only if the prior art had had the guidance of the present concepts of the present lnventlon; and the prlor art had much motl~ation for the prPsent invention~
~ ha-t ie, lt le emphasizèd that the prior art had eeveral par-ticular~ of prior art and motivation which lndividually and accumulatively show the non-obviou~neee of thi~ combination invention a~ to lts variou~ featuree:
~728fi9 Tubea, tublng, and varlous piping installat~ons are device~ which are of ancient use and knswledge, even tubing for use ln many types of medical therapy, and specificall~
including tubing harneases ~or rezpiration ass1etance ~nd re~piration monitoring; and such tubing and tubing fittlnga, including those o~ flexibl~ material, have been used by ~n untold numbers D~ persons, the world over.
Further non-obviousness of the lnvention is shown by the fact that ~lttlngs for tubl~g have been made from material having flexibility, and by plastlc molding pro~edures which have provided ahoulders and other changea Or diameter, etc~
With the re~lity oi Al l these ~actor~, the inventive non-obviou~ness of the present lnvention i~ quite manifest.
IV The prior art has had f~aturea of the ~reaent invention, an _approac es o ~ concep 8~ u no n ~ com ina lon b~ w lch the lnventlon as a whoIë~l~a~advant~eou~ achieved:
The background of prior art a~ ~ust aummarlzed ~eems more ~lgnificant in showing the nonobviousnes3 oi' the pre~ent concepts whe~ alao it i9 reminded that the prior art also had - 2~72~9 and used princlplas of ln~ertabillty in dlverae a~d lnnumerable aa~e~bly procedures.
Moreover, materlals having conaiderable flexibility are of course qulte well known, and known in èven UBa~ of medlcal equipment Or various natures.
Molding and other manufacturing procedure0 are well known by which ~11 components of the pre~ent invention could be made.
Joined and/or ~oinabl~ fittlng~ for hoaea and tubing are also krown in the prior art.
~ he prior art haa tried a variety of types of re~piratory harnes~es, and tubing for each of o~ygen supply and for monitorlng the breathlng cycles. And the existence of ~uch articlee embodying such varioua features is not only conceded, it 1~ emphaeized; for a~ to the novelty here of 20~2~
the combin~tion, of the inventlon a~ consldered a~ a whole, ~ contraat to the prior art helps ~how both the great variety and the dlssatisfaction of the various prlor art attempts of improvement, and the advantag ~ and the lnventive ~ignificance of thQ pre~ent concepts. lhua, as shown herein as a contrast to all the prior art, the lnventlve significanca of the pre~ent concepts as a comblnation is emphaaized, and the nature of the concepts and their resulta can perhaps be easier understood.
Although ~arietles of prior art ars conceded, end ample motl~ation i8 shown, and full capabllity in the prior art i~
conceded, no prior art ~howR or Huggests details of the overall combinatior~of the pre~ent lnvention, as la the proper and acce/pted wa~ oY consldering the inventiveneas nature of the concepts.
~ hat ia, although the prior art ahows an approach to the overall invention, of tubing for oxygen-supply and for monitoring, and the prior art has shown varlous natures of tubing and flttings, including flexibllity, etc., it i9 aignifirant that none o~ the prior art RhowH the novel and advantageou~ combination, which provld~ the merits of this invention, aven though certain detalls are shown ~eparately from this accompllshment.
2~7~86~
Accordingly, the ~arious concept~ and components are conceded and emphaaized to have been widely known in the prior art as to variou~ device~; neverthele~s, the prior art not having had the particular co~bination of concepta and details aa here presented and shown in no~el combination dlfferent from the prior art and itB suggeation~, even only a fair amount of realistlc humllity, to avoid coneideration o~ this invention lmproperly by hind~ight, requlres the concepts and achievements here to be realistically vlewed a~ a novel combinations,ln~entive in nature And especially is this 2 realistic consideration when viewed from the position o~ a person of ordinary skill in this art at the time of this invention, and without trying to reconstruct this invention from the prior art without use of hindsight toward particulzrs not suggested by the ~rior art of all rele~ant field~. .
V. 8rie description of the Drawin~s:
The above de~crlption o`f the novel and advantageous invention is of somewhat introductory and generalized form.
More particular details, conceptq, and features are set forth in the following and more detaiied descr~ption of an 2~728sg ll llluetrative emb~diment, reference being had to the accompanying aomewhat achematlc drawings, ln which:
Fig. 1 la an overall vlew of a cannula harness having a dual lumen cannula pair according to the present invention;
Fig. 2 i~ an snlarged cross-sectionPl view of the hosea or tubing used in the device of ~ig. 1, shown generally Q9 taken by gection-line 2-2 of Flg. l;
Fig. 3 and 4 are exterior views of an inner hosa fitting and an outer hose fltting, re~pectively, which in their asae~bly provide an overall body member as shown in Fig. 5; and Fig. 5, in enlarged Bcale~ i8 an axlal cross-3ectional view of the assembl~ of the flttings of Fig. 3 and 4, each of the two cannulae providing a generally concentric pair of bores reapectively communicating with one of the hosea of Fig. 1, with and f!rRgments of those hosea shown as connected reapectively tot`~oee flttings.
VI. Detalled de~criptlon of the illu~tr.ative embodiment:
As shown in the drawlnga, the in~ention provides cannula apparatu3 10 for providing modified re3piration to a patient, and the monitoring o~ the reapiration of the patient-2~7~
More partlcularly, ~uch cannula apparstus 10 in atypical use is for use with aasociated ~upply equ1pment~
auch a~ o~ygen-~upply equlpment (~hown diagrammatically at 12) for the provlding of a supply o~ as~ociated gas ~uch ae o~ygen for the provlding of modified re~piration; and the cannula apparatus 10 a~ shown is typically u~ed also, and concurrently, with as~ociated control equlpment 14 for controlling the a~sociated ga~ supply equipment 12, corresponding to the monitoring function, and thereby controlling the delivery of tha as60clated ga~ to the can~ula apparatus 10~ (The control equipment 14 1 e also shown merely disgrammatically.) In the typical use of an o~ygen or oxygen/air supply nnd ~ breathlng-monitor function, as in Fig. 1, the a~sociatad equipment 12 i~ shown as provided with a gaa delivery hoss 16, and the monitor equipment 14 i~ shown provided with a monitoring hoee 18, schematically shown as respectively conneoted to and communicating wlth the gas ~upply 12 end the monitored control equipment 14.
The hoses or tubing 16/18 are desirably of a "peel-apart"
type, and typically a~ shown will be of identical size, both as to inside diameter and out~ide diP~eter.
Turning now to the invention particulars, the cannula apparatus 10, not considerlng the ho~es 1~/18, compri~es an 2~72~
aseembly 20 of a palr of generall~ cylindrical body members here ehown as a first (or "outer" for reasons apparent below) body ~ember 22 and a aecond (or "inner" ~or rea~ons apparent below) body member 24; and it is by the aasembly 20 of the~e member~ 22/24 that the pair of dual lumen cannulae are provlded.
Each of the first body member 22 and the ~econd body member 24 has a generally hollow primary bore, re~pectively 26 and 28, and are respectively provided with an inlet respectlvely 30 and 32 communicating the respect1ve prlmary bore 26/28 with one of the reepecti~e gaa delivery hoee 16 and monltoring ho~e 18.
Each of the primary borea 26/Z8 al90 i9 shown aa having a pair of outleta, re~pectively 34 and 36, each palr of those outlets 34 and 36 belng corre~pondingly ~paced, thus regietering when the fittings 22/24 are as~embled, as ~hown in Fig. 5.
The fir~t or outer body member 22 is provided with two cannula nipple~ 38, each having a generally hollow secondary lumen or bore 40; and each of the secondary bore~ 40 of the cannula nipple~ 38 or the first or outer body member 22 hae an inlet 42 end an outlet 44; and the inlet 42 of the ~eco~dary bore~ 40 o~ the two cannula nipples 38 or the first body member 22 communlcates directly with a re~pective one of the 2~728~9 ou-tlet~ 34 of the prlmary bore 26 o~ the ~ir~t body member 22.
~ hs second or inner bod~ member 24 ia quite similar to the flrat or outer body member 22, a~ now particularized and as apparent from the drawings.
~ hat i~, the aecond or inner body member 24 ia provided wlth two cannula nipple~ 46 each having a generally hollow eecondary lumen or bore 48, each of the secondary boree 48 o~
the cannula nipple3 46 of th~ aecond or inner body member 24 having an inlet 50 and an outlet 52.
Similarly to thoee of the firat body member 22, the inlet 50 of the secondary borea 48 of the two cannula nipple~ 46 of the 0econd or inner body member 24 communicate~ directly with a reapective ons of the outleta 36 of the primary bore 28 of the ~econd or lnner body member 24.
As also ahown be~t in Fig. 5, the pair of cannula nipple~ 38 of the first or outer body member 22 and the pair of cannula nipples 46 of the ~econd or inner body memb~r 24 are corre~pondingly spaced; and the portion of the ~econd body member 24 having the two outlet~ 36 o~ lts primary bore 28 i~ located within the pr~mary bore 26 of the first or outer body membsr 22,a~d, when a~gem~led ag in Flg. 5, the cannula nipple~ 46 o~ the ~scond or inner body member 24 are located within the ~econdary bore 40 o~ the respective cannula nipple3 38 2~72~9 of the firat or outer body member 22.
lhe spaclng of the aets of cannulae 38/46 1~ qulte short, i.e., JUBt enough to straddle the cartilage between a per~on's no~trlls for the insertion of the cannulae 38 containing the cannu~ae 46; and the transverse length of the cannulae 38/46 ~e anown in Fig. 5 ie 6uch that whe~ the fitting~ 22/24 are as~embled they end in a common plane~
Assembly to the condition of ~ig. 5 is achie~ed by providing that the cannula nipplea o~ the second or inner body member 24 are provided to be sufficiently resiliently Ylexlble that the second body member 24 may be assembled lnto the primary bore 26 of the first body member 22,and the cannula nipples 46 of the 3econd body member 24 assembled into the secondary bore 40 of the respective cannula nipples 38 of the flrat body member 22, by relatively pushlng the aecond body member 24, axl~lly of the primary bore 26 of ~he first body member 22, into the primary bore 26 oY the flr3t body m~mber 22.
In such asaembly, the flexibility accommodate6 the flexing and bending of the cannulae 46 of the second body member 24 during the lnaertion; and the reailience cau~e3 them to epring into the fiecondary borea 40 of the cannulae 38 of the first body member~ aa Bhown in Fig. 5 as a~aembled.
2~728~9 The accommodatlon of interchangeability i8 now explained.
That 18, the cros~-sectional area of the primary bore 28 of the ~econd body member 24 i~ operatively the same a~ the dif~erence between the cro~ ectional area of the primary bore 26 of the firat body member 22 and the cross-~ectional area of the outer portion 56 o~ the ~econd body member 24 ~hat operatiYe eameness of cro~s-~ectional areas provides that it i8 a matter of substantial indifference which of the fir~t or outer body member'e inlet 30,or eecond or inner body member's inlet 32,i~ operatively connected to the gas delivery ho~e 16 or the monitoring ho~e 18.
Slmilarly providlng that interchangeability ie the araa con~ideration of the aete of a~embled cannulae 38/46 snd 38/46.
More particularly, that i8, ae t;o each pair of cannula nipples 38 of the flrct body member 22 and of nipples 46 of the ~econd body member 24, the cro~e-eectional area oX the secondary bore 48 of each cannula nipple 46 of the ~econd or inner body member 24 i~ operatlvel~ the same as the difforence between the croae-~ection~l area oi the secondary bore 40 of the respective cannula nipple ~8 of the flrst or outer body member 22 and the cro~s-eectional area of the outer portion 58 of the oannula nipple 46 of the eecond b~dy mamber 24.
~072~69 That relatlonahlp, of an operat~ve sameneaa of cross-asctlonal areaa,alao provide~ that it i~ a matter o~ ~ubstantlal indifference which o~ the fir~t body memberl~ inlet 30 or ~econd body ~e~ber'~ inlet 32 iB operatively ¢onnected to the ga~ delivery hoae 16 or the monitoring hose 18.
(The word "operative", as used with respect to the croa~-sectional areaa mentionedJ considers not only rea~onable dlmensional tolerances but the factor that fluid flow and/or re~triction i8 a ~unction of wall area aa well as open area.) The cannula apparatuc lO thu~ provide~ a cannula nipple ~8/46 with a dual outlet 44~52 for each of a person'~ no~trll~, in proximity to one another, for both deliverlng ga~ to each of the person'~ nostril~, and monitoring the respiration of the perDon by monltoring the re~piration a~ to each of the peraon's nostril~. And, interchangeability i8 also achieved, as de~crlbed herein.
VII. Other detail~, and a _mary ac to uae:
The operativity ahould be mani~e~t by the drawin~s and the above de~criptlon~ That i8, the ~lexibllity of the lnner fitting or ~econd body member 24, and particularly of its transverse cannula nipples 46, permit~ it to be pushed axially (rightwardly, ~ig. 5) into the downatream a~ial outlet 60 2~728~9 of the outer fitting or firat body member 22; and cannula nlpples 46 of the inner body member 24 then spring into the reapective bores or lumen~ 40 of the tranaverse cannula nipples 38 of the outer fitting 22 as per Fig. 5. (The downs-tream and of the bore 28 of body member 24 i9 shown cloaed, at 61.) Ccnvenien~e i8 further achlé~ed by operati~e equslity of ~low area~ aH apecified, making it indifferent as to which of the tubing seotiona 16 and 18 are connected to the Gxygen-supply equipment or breathing monitoring equipment, or, similarly, to which of the tublng sections 16 and 18 it iB that each of the inner fitting 22 or outar fitting 24 body members are connected.
Also, accommodating an. interchange of fittinge 22 and 24, snd hose~ 16 and 18, it wlll be noted that tha upstream cylindrical end portions 30 and 32 of both fittinga 22 and 24 are o~ the same lnner dlameter~ they both being ahown aa receased or counterbored (62) to reCeilTe the hosea 16~
all.~hown the same diameter aa the bore 28 of body member 24.
~ he outer ~houlder64 on the inner fitting 24, ad~acent lta upatream end 65, providea a atop 66 against which the down~tream end 60 of the outer fittlng 22 is pushed, assuring a length o~ clcaure engagement of the inner cylindrlcal wall 68 2072~
of the downstream end 60 of the outer fltting 24 again~t ths outer ~urface 70 of the rai~ed or enlarged di~meter portlon 72 of the inner ~itting 24 ~ust down~tream of that lnner ~itting Mhoulder 64 ad~acent ita upatream end 65.
If two gasea "A" and "~" are to be supplied in~tsad of one boine a monitoring line, for brevlty it i8 mentioned merely that the same embodlment is illu~trative, except that llno 18 would be another gas line, with equlpment 14 being that of that gaa ~upply line; but the description including interchangeability of ~itting 22/24 and/or tubing lines 16/18 appl~es as above deacribed.
VIII. Conclusion:
It is thus ~een that a cannula harne~a or the like, provided and used according to the invenl;ive concepts herein aet forth, provides novel concepts of a cle~irable and advantageoua device, yielding the advantages of an o~erall combination of respiration equipment providing Q pair of lumena for each of two cannulae, interchangeably useful for providing a ga~ and a monitor, or two gases, particularlr for respiration-as~isted therapy, which, in overall combination, le conceptually different 2~17286~
from the prior art even t~ough objects embodying certain of the mechanical detail~ a~ a baaic capability have o~ course been known for year~ yet eignlficantly this particular combination, even consldered as lncluding prior art concept~, has not been suggebted by the prior art, this achievement being a substantial and advantageous departure from prior art, even though the prior art shows attempts at lmprovement and variations as to oxygen therapy and other respiration-a~si~ted therapy for many year~.
~nd particularly ia the overall diference ~rom the prior art significant when the non-obviousness is viewed by a consideration of the subject ~atter as a whole, as integrally incorporating a combination of features aa different from the prior art, in contrast to merely those details of novelty -theMselves, and further in view of the prlor art teaching awa~ from the particular and inter-related concepts and feature8 of the pre8ent ~nvention.
In summary a~ to the nature oE the~e advantageous concepts, their inventiveness is showm by novel features of concept and construction shown here, in novel and advantageous combination, not only being different from all the prior art known, but because the achievement 2~28~
is not what is or has been suggested to those of ordinary sklll in the art, e~pecially reali~tlcally considerlng thls a~ comprising components whioh lndividually are eimilar in nature to what ia well known to makers and users of respiration-aaai8tlng tublng for mang ~ear3. No prior art hae suggeated the modificatlons oi any prior art to achieve the novel concepta here achieved, with the varloua features providing their own functions in the overall comblnation.
Accordlngly, it will thus be seen from the foregoirg description of the invention according to this illu~trative embodiment, considered with the accompanying drawinga, that the preaent in~ention provides new and useful concepts of a novel and advantageous reaplration-assiat~g devlc3 having and yielding deaired advantages and characteriatlc~ in formation and uae, and accomplishlng the intended ob~ects, lncluding thoae here~nbefore polnted out and others which are inherent in the invention.
~7~8~
Modifications and variations may be effected without departln~ from the scope of the novel concept~ of the invention; accordingly, the invention is not limlted to the specific embodiment/ or form or arran~ement of part~
herein described or sho~l,
Dual ~umen Cannula I. Field of the Invention-.
This invention relatea to respiration therapy, and more particularly to re~piration therapy in which a gas (usually oxygen or an oxygen/alr mixture) i~ to be dellvered into a patient's noatril~ by ~ome aort of a cannula inaerted into the patient'a no~e, and a breathlng-monitoring cannula le ~lao needed in close proximity to control details of the ov~rall reapiration-therapy equipment and procedure.
Such detalls, i.e., of breathing-monitoring, control of preaaure and ~upply of the resplration gas, sequential setting of the respiratlon equipment components, etc., are not part of this invention, but they are mentioned to indlcate th0 reason for the breathing~monitoring functibn to be needed;
and ~ince that breathing-monitoring fu~ction i~ needed, that is the reason why breathing-monitoring cannulae are needed in the patient~a nose even though the preaence of an e~tra cannula in each noatril is a aource of extra bother and discomfort to the patient, who is likely to find any sort of respiration therapy disagreeable to aay the lea~t.
2~7~8~
With auch reepiratlon therapy, therefOre~ the presence of two cannulae has long been known to be needed~ ln a dual arrangement providing a pair of cannulae and thelr gaa-delivery or monitoring bores (lumena) ln a eort of harne~a, with one tube going to the oxygen or air/oxygen supply, and one tube connected to either some monltor/control equipment or to another ga~.
Again~t that background, the present invention's achlevements are to provide better patient comfort, ease ~d convenience for the attendant, good operativlty, etc.
II. ~ummary of the Invention:
In carrying out the lnvention, there are provided a pair of body members, one being an inner one and one being an outer one, each havlng a primary bore and a apaced pair of cannula nipplea.
One of the oannula nipplee oE the outer body member, and one of the cannula nlpplee of the inner bod~ member, reapectively, are provided as a ~et, for each of a per~onls noetril~; and each set provides for one of the body members 2~2~9 a respiratlon gas and either a monitorlng of that gas or a supply of a dlfferent gas.
~ he cannula nipplea o~ the inner body member are made to be sui'ficlently fle~ible, preferably by the inner body memb~r being formed integrally with its cannula nipples~
all from a fle~ible material, that aasembly i~ aohleved by pushing the lnner body lnto an open end of the outer body;
and thie flexibllity accommodates assembly even though the nipplea of both body members extend transver~ely of the portlon of the Oody me~ber haYing its primary bore.
Interchangeability of either the inner body member and outer body member provldes for convenience of use; and thia lnterchangeabllity is achieved by providing all corresponding portlona of the inner and outer body ~ember~ o~ operatively equal cross-~ectlonal bore areas, i.e., the croaa-aectional area of the inner body memb~r is operatively equal to the cross-sectlonal area of the outer body member minu~ the cross-sectional area of the outer surface o~ the inner body member.
2072~6~
III. The prior art doe~ not show the inventive concepts, even though patlen~-theraEy~h~ long ~lIized--modi~led re~PlratlOn uein~ cannulae:
The prior art therapy has long provided var$ous modifications of human respiration, particularly oxygen and or ox~gen/air mlxtures; and, since it has been long known that the supply and rate of oxygen delivery to the patient must be kept within prescrlbed limita, and since ~upply-control equipment ha~ been provided which sen~es re~piration a~ a mean~ of economi~ing the oxygen delivery, the prior art ha~ provided not only an oxygen-supply tube arrangement but also a re~piration-monltoring tube to control the oxygen supply.
And sinoe humans have two no~trils, and since the re~piration o~ the two noatrils is often slgnificantly different, the prior art has provlded both an oxygen-supply tube and a breath-monitoring tube for each nos-tril.
Yet not only is oxygen therapy itself bothersome and annoying to many patient~ the e~tra monitoring tube u~e, 2~2869 making two tubes for each nostril, all accumulate to make oxygen therapy of additional di6comfort to the patient, especially of cour~e with the other discomforts of the therapy environment and ~ituation, The prlor art has provided monitoring equipment for monitoring the respiration cycle of a patient (inhaling, dwell, and exhaling periods) 80 aa to cause the oxygen or oxygen~air to be forced to the patient only at certain periods of the cycle (for both patient-comfort and oxygen economy);
and that monitoring has been provided by tubing whose open or ~en~ing end i~ in close proximity to the oxygen or oxygen/alr outlet.
It has apparently seemed inevitable to the prior art~
or at least an inherent lncident of oxygen 3upply and breath-monltoring,that ~eparate tube~ be pro~ided for the oxygen-3upply and for the breath-monitoring operativity for each nostril, and that each of the set for each nostril be kept eeparate to avoid undue masking of the resplration by the oxygen supply.
2~7~9 With thls background, the ~ignificance of the pre~ent invention, by which the patlent la required to be bothered by only a ~ingle cannula nlpple in each noetril, i8 better eeen to be quite advantageous, making tha oxygen therapy le~
bothersome and more endurable.
In a hindsight consideration ofthe present invention to determine its inventive and novel nature, it is not only conceded but emphasized that the prior art had details usable in this invention but only if the prior art had had the guidance of the present concepts of the present lnventlon; and the prlor art had much motl~ation for the prPsent invention~
~ ha-t ie, lt le emphasizèd that the prior art had eeveral par-ticular~ of prior art and motivation which lndividually and accumulatively show the non-obviou~neee of thi~ combination invention a~ to lts variou~ featuree:
~728fi9 Tubea, tublng, and varlous piping installat~ons are device~ which are of ancient use and knswledge, even tubing for use ln many types of medical therapy, and specificall~
including tubing harneases ~or rezpiration ass1etance ~nd re~piration monitoring; and such tubing and tubing fittlnga, including those o~ flexibl~ material, have been used by ~n untold numbers D~ persons, the world over.
Further non-obviousness of the lnvention is shown by the fact that ~lttlngs for tubl~g have been made from material having flexibility, and by plastlc molding pro~edures which have provided ahoulders and other changea Or diameter, etc~
With the re~lity oi Al l these ~actor~, the inventive non-obviou~ness of the present lnvention i~ quite manifest.
IV The prior art has had f~aturea of the ~reaent invention, an _approac es o ~ concep 8~ u no n ~ com ina lon b~ w lch the lnventlon as a whoIë~l~a~advant~eou~ achieved:
The background of prior art a~ ~ust aummarlzed ~eems more ~lgnificant in showing the nonobviousnes3 oi' the pre~ent concepts whe~ alao it i9 reminded that the prior art also had - 2~72~9 and used princlplas of ln~ertabillty in dlverae a~d lnnumerable aa~e~bly procedures.
Moreover, materlals having conaiderable flexibility are of course qulte well known, and known in èven UBa~ of medlcal equipment Or various natures.
Molding and other manufacturing procedure0 are well known by which ~11 components of the pre~ent invention could be made.
Joined and/or ~oinabl~ fittlng~ for hoaea and tubing are also krown in the prior art.
~ he prior art haa tried a variety of types of re~piratory harnes~es, and tubing for each of o~ygen supply and for monitorlng the breathlng cycles. And the existence of ~uch articlee embodying such varioua features is not only conceded, it 1~ emphaeized; for a~ to the novelty here of 20~2~
the combin~tion, of the inventlon a~ consldered a~ a whole, ~ contraat to the prior art helps ~how both the great variety and the dlssatisfaction of the various prlor art attempts of improvement, and the advantag ~ and the lnventive ~ignificance of thQ pre~ent concepts. lhua, as shown herein as a contrast to all the prior art, the lnventlve significanca of the pre~ent concepts as a comblnation is emphaaized, and the nature of the concepts and their resulta can perhaps be easier understood.
Although ~arietles of prior art ars conceded, end ample motl~ation i8 shown, and full capabllity in the prior art i~
conceded, no prior art ~howR or Huggests details of the overall combinatior~of the pre~ent lnvention, as la the proper and acce/pted wa~ oY consldering the inventiveneas nature of the concepts.
~ hat ia, although the prior art ahows an approach to the overall invention, of tubing for oxygen-supply and for monitoring, and the prior art has shown varlous natures of tubing and flttings, including flexibllity, etc., it i9 aignifirant that none o~ the prior art RhowH the novel and advantageou~ combination, which provld~ the merits of this invention, aven though certain detalls are shown ~eparately from this accompllshment.
2~7~86~
Accordingly, the ~arious concept~ and components are conceded and emphaaized to have been widely known in the prior art as to variou~ device~; neverthele~s, the prior art not having had the particular co~bination of concepta and details aa here presented and shown in no~el combination dlfferent from the prior art and itB suggeation~, even only a fair amount of realistlc humllity, to avoid coneideration o~ this invention lmproperly by hind~ight, requlres the concepts and achievements here to be realistically vlewed a~ a novel combinations,ln~entive in nature And especially is this 2 realistic consideration when viewed from the position o~ a person of ordinary skill in this art at the time of this invention, and without trying to reconstruct this invention from the prior art without use of hindsight toward particulzrs not suggested by the ~rior art of all rele~ant field~. .
V. 8rie description of the Drawin~s:
The above de~crlption o`f the novel and advantageous invention is of somewhat introductory and generalized form.
More particular details, conceptq, and features are set forth in the following and more detaiied descr~ption of an 2~728sg ll llluetrative emb~diment, reference being had to the accompanying aomewhat achematlc drawings, ln which:
Fig. 1 la an overall vlew of a cannula harness having a dual lumen cannula pair according to the present invention;
Fig. 2 i~ an snlarged cross-sectionPl view of the hosea or tubing used in the device of ~ig. 1, shown generally Q9 taken by gection-line 2-2 of Flg. l;
Fig. 3 and 4 are exterior views of an inner hosa fitting and an outer hose fltting, re~pectively, which in their asae~bly provide an overall body member as shown in Fig. 5; and Fig. 5, in enlarged Bcale~ i8 an axlal cross-3ectional view of the assembl~ of the flttings of Fig. 3 and 4, each of the two cannulae providing a generally concentric pair of bores reapectively communicating with one of the hosea of Fig. 1, with and f!rRgments of those hosea shown as connected reapectively tot`~oee flttings.
VI. Detalled de~criptlon of the illu~tr.ative embodiment:
As shown in the drawlnga, the in~ention provides cannula apparatu3 10 for providing modified re3piration to a patient, and the monitoring o~ the reapiration of the patient-2~7~
More partlcularly, ~uch cannula apparstus 10 in atypical use is for use with aasociated ~upply equ1pment~
auch a~ o~ygen-~upply equlpment (~hown diagrammatically at 12) for the provlding of a supply o~ as~ociated gas ~uch ae o~ygen for the provlding of modified re~piration; and the cannula apparatus 10 a~ shown is typically u~ed also, and concurrently, with as~ociated control equlpment 14 for controlling the a~sociated ga~ supply equipment 12, corresponding to the monitoring function, and thereby controlling the delivery of tha as60clated ga~ to the can~ula apparatus 10~ (The control equipment 14 1 e also shown merely disgrammatically.) In the typical use of an o~ygen or oxygen/air supply nnd ~ breathlng-monitor function, as in Fig. 1, the a~sociatad equipment 12 i~ shown as provided with a gaa delivery hoss 16, and the monitor equipment 14 i~ shown provided with a monitoring hoee 18, schematically shown as respectively conneoted to and communicating wlth the gas ~upply 12 end the monitored control equipment 14.
The hoses or tubing 16/18 are desirably of a "peel-apart"
type, and typically a~ shown will be of identical size, both as to inside diameter and out~ide diP~eter.
Turning now to the invention particulars, the cannula apparatus 10, not considerlng the ho~es 1~/18, compri~es an 2~72~
aseembly 20 of a palr of generall~ cylindrical body members here ehown as a first (or "outer" for reasons apparent below) body ~ember 22 and a aecond (or "inner" ~or rea~ons apparent below) body member 24; and it is by the aasembly 20 of the~e member~ 22/24 that the pair of dual lumen cannulae are provlded.
Each of the first body member 22 and the ~econd body member 24 has a generally hollow primary bore, re~pectively 26 and 28, and are respectively provided with an inlet respectlvely 30 and 32 communicating the respect1ve prlmary bore 26/28 with one of the reepecti~e gaa delivery hoee 16 and monltoring ho~e 18.
Each of the primary borea 26/Z8 al90 i9 shown aa having a pair of outleta, re~pectively 34 and 36, each palr of those outlets 34 and 36 belng corre~pondingly ~paced, thus regietering when the fittings 22/24 are as~embled, as ~hown in Fig. 5.
The fir~t or outer body member 22 is provided with two cannula nipple~ 38, each having a generally hollow secondary lumen or bore 40; and each of the secondary bore~ 40 of the cannula nipple~ 38 or the first or outer body member 22 hae an inlet 42 end an outlet 44; and the inlet 42 of the ~eco~dary bore~ 40 o~ the two cannula nipples 38 or the first body member 22 communlcates directly with a re~pective one of the 2~728~9 ou-tlet~ 34 of the prlmary bore 26 o~ the ~ir~t body member 22.
~ hs second or inner bod~ member 24 ia quite similar to the flrat or outer body member 22, a~ now particularized and as apparent from the drawings.
~ hat i~, the aecond or inner body member 24 ia provided wlth two cannula nipple~ 46 each having a generally hollow eecondary lumen or bore 48, each of the secondary boree 48 o~
the cannula nipple3 46 of th~ aecond or inner body member 24 having an inlet 50 and an outlet 52.
Similarly to thoee of the firat body member 22, the inlet 50 of the secondary borea 48 of the two cannula nipple~ 46 of the 0econd or inner body member 24 communicate~ directly with a reapective ons of the outleta 36 of the primary bore 28 of the ~econd or lnner body member 24.
As also ahown be~t in Fig. 5, the pair of cannula nipple~ 38 of the first or outer body member 22 and the pair of cannula nipples 46 of the ~econd or inner body memb~r 24 are corre~pondingly spaced; and the portion of the ~econd body member 24 having the two outlet~ 36 o~ lts primary bore 28 i~ located within the pr~mary bore 26 of the first or outer body membsr 22,a~d, when a~gem~led ag in Flg. 5, the cannula nipple~ 46 o~ the ~scond or inner body member 24 are located within the ~econdary bore 40 o~ the respective cannula nipple3 38 2~72~9 of the firat or outer body member 22.
lhe spaclng of the aets of cannulae 38/46 1~ qulte short, i.e., JUBt enough to straddle the cartilage between a per~on's no~trlls for the insertion of the cannulae 38 containing the cannu~ae 46; and the transverse length of the cannulae 38/46 ~e anown in Fig. 5 ie 6uch that whe~ the fitting~ 22/24 are as~embled they end in a common plane~
Assembly to the condition of ~ig. 5 is achie~ed by providing that the cannula nipplea o~ the second or inner body member 24 are provided to be sufficiently resiliently Ylexlble that the second body member 24 may be assembled lnto the primary bore 26 of the first body member 22,and the cannula nipples 46 of the 3econd body member 24 assembled into the secondary bore 40 of the respective cannula nipples 38 of the flrat body member 22, by relatively pushlng the aecond body member 24, axl~lly of the primary bore 26 of ~he first body member 22, into the primary bore 26 oY the flr3t body m~mber 22.
In such asaembly, the flexibility accommodate6 the flexing and bending of the cannulae 46 of the second body member 24 during the lnaertion; and the reailience cau~e3 them to epring into the fiecondary borea 40 of the cannulae 38 of the first body member~ aa Bhown in Fig. 5 as a~aembled.
2~728~9 The accommodatlon of interchangeability i8 now explained.
That 18, the cros~-sectional area of the primary bore 28 of the ~econd body member 24 i~ operatively the same a~ the dif~erence between the cro~ ectional area of the primary bore 26 of the firat body member 22 and the cross-~ectional area of the outer portion 56 o~ the ~econd body member 24 ~hat operatiYe eameness of cro~s-~ectional areas provides that it i8 a matter of substantial indifference which of the fir~t or outer body member'e inlet 30,or eecond or inner body member's inlet 32,i~ operatively connected to the gas delivery ho~e 16 or the monitoring ho~e 18.
Slmilarly providlng that interchangeability ie the araa con~ideration of the aete of a~embled cannulae 38/46 snd 38/46.
More particularly, that i8, ae t;o each pair of cannula nipples 38 of the flrct body member 22 and of nipples 46 of the ~econd body member 24, the cro~e-eectional area oX the secondary bore 48 of each cannula nipple 46 of the ~econd or inner body member 24 i~ operatlvel~ the same as the difforence between the croae-~ection~l area oi the secondary bore 40 of the respective cannula nipple ~8 of the flrst or outer body member 22 and the cro~s-eectional area of the outer portion 58 of the oannula nipple 46 of the eecond b~dy mamber 24.
~072~69 That relatlonahlp, of an operat~ve sameneaa of cross-asctlonal areaa,alao provide~ that it i~ a matter o~ ~ubstantlal indifference which o~ the fir~t body memberl~ inlet 30 or ~econd body ~e~ber'~ inlet 32 iB operatively ¢onnected to the ga~ delivery hoae 16 or the monitoring hose 18.
(The word "operative", as used with respect to the croa~-sectional areaa mentionedJ considers not only rea~onable dlmensional tolerances but the factor that fluid flow and/or re~triction i8 a ~unction of wall area aa well as open area.) The cannula apparatuc lO thu~ provide~ a cannula nipple ~8/46 with a dual outlet 44~52 for each of a person'~ no~trll~, in proximity to one another, for both deliverlng ga~ to each of the person'~ nostril~, and monitoring the respiration of the perDon by monltoring the re~piration a~ to each of the peraon's nostril~. And, interchangeability i8 also achieved, as de~crlbed herein.
VII. Other detail~, and a _mary ac to uae:
The operativity ahould be mani~e~t by the drawin~s and the above de~criptlon~ That i8, the ~lexibllity of the lnner fitting or ~econd body member 24, and particularly of its transverse cannula nipples 46, permit~ it to be pushed axially (rightwardly, ~ig. 5) into the downatream a~ial outlet 60 2~728~9 of the outer fitting or firat body member 22; and cannula nlpples 46 of the inner body member 24 then spring into the reapective bores or lumen~ 40 of the tranaverse cannula nipples 38 of the outer fitting 22 as per Fig. 5. (The downs-tream and of the bore 28 of body member 24 i9 shown cloaed, at 61.) Ccnvenien~e i8 further achlé~ed by operati~e equslity of ~low area~ aH apecified, making it indifferent as to which of the tubing seotiona 16 and 18 are connected to the Gxygen-supply equipment or breathing monitoring equipment, or, similarly, to which of the tublng sections 16 and 18 it iB that each of the inner fitting 22 or outar fitting 24 body members are connected.
Also, accommodating an. interchange of fittinge 22 and 24, snd hose~ 16 and 18, it wlll be noted that tha upstream cylindrical end portions 30 and 32 of both fittinga 22 and 24 are o~ the same lnner dlameter~ they both being ahown aa receased or counterbored (62) to reCeilTe the hosea 16~
all.~hown the same diameter aa the bore 28 of body member 24.
~ he outer ~houlder64 on the inner fitting 24, ad~acent lta upatream end 65, providea a atop 66 against which the down~tream end 60 of the outer fittlng 22 is pushed, assuring a length o~ clcaure engagement of the inner cylindrlcal wall 68 2072~
of the downstream end 60 of the outer fltting 24 again~t ths outer ~urface 70 of the rai~ed or enlarged di~meter portlon 72 of the inner ~itting 24 ~ust down~tream of that lnner ~itting Mhoulder 64 ad~acent ita upatream end 65.
If two gasea "A" and "~" are to be supplied in~tsad of one boine a monitoring line, for brevlty it i8 mentioned merely that the same embodlment is illu~trative, except that llno 18 would be another gas line, with equlpment 14 being that of that gaa ~upply line; but the description including interchangeability of ~itting 22/24 and/or tubing lines 16/18 appl~es as above deacribed.
VIII. Conclusion:
It is thus ~een that a cannula harne~a or the like, provided and used according to the invenl;ive concepts herein aet forth, provides novel concepts of a cle~irable and advantageoua device, yielding the advantages of an o~erall combination of respiration equipment providing Q pair of lumena for each of two cannulae, interchangeably useful for providing a ga~ and a monitor, or two gases, particularlr for respiration-as~isted therapy, which, in overall combination, le conceptually different 2~17286~
from the prior art even t~ough objects embodying certain of the mechanical detail~ a~ a baaic capability have o~ course been known for year~ yet eignlficantly this particular combination, even consldered as lncluding prior art concept~, has not been suggebted by the prior art, this achievement being a substantial and advantageous departure from prior art, even though the prior art shows attempts at lmprovement and variations as to oxygen therapy and other respiration-a~si~ted therapy for many year~.
~nd particularly ia the overall diference ~rom the prior art significant when the non-obviousness is viewed by a consideration of the subject ~atter as a whole, as integrally incorporating a combination of features aa different from the prior art, in contrast to merely those details of novelty -theMselves, and further in view of the prlor art teaching awa~ from the particular and inter-related concepts and feature8 of the pre8ent ~nvention.
In summary a~ to the nature oE the~e advantageous concepts, their inventiveness is showm by novel features of concept and construction shown here, in novel and advantageous combination, not only being different from all the prior art known, but because the achievement 2~28~
is not what is or has been suggested to those of ordinary sklll in the art, e~pecially reali~tlcally considerlng thls a~ comprising components whioh lndividually are eimilar in nature to what ia well known to makers and users of respiration-aaai8tlng tublng for mang ~ear3. No prior art hae suggeated the modificatlons oi any prior art to achieve the novel concepta here achieved, with the varloua features providing their own functions in the overall comblnation.
Accordlngly, it will thus be seen from the foregoirg description of the invention according to this illu~trative embodiment, considered with the accompanying drawinga, that the preaent in~ention provides new and useful concepts of a novel and advantageous reaplration-assiat~g devlc3 having and yielding deaired advantages and characteriatlc~ in formation and uae, and accomplishlng the intended ob~ects, lncluding thoae here~nbefore polnted out and others which are inherent in the invention.
~7~8~
Modifications and variations may be effected without departln~ from the scope of the novel concept~ of the invention; accordingly, the invention is not limlted to the specific embodiment/ or form or arran~ement of part~
herein described or sho~l,
Claims (14)
1. Cannula apparatus providing for modified respiration and the monitoring thereof as to a human patient, for use with (a) associated supply equipment for the providing of a supply of associated gas for providing the modified respiration, and with (b) associated control equipment for controlling the associated supply equipment and thereby controlling the delivery of the associated gas to the cannula apparatus, the associated equipment being provided with a gas delivery hose and a monitoring hose, respectively for communication with the gas supply and the control equipment;
the cannula apparatus comprising:
a first body member and a second body member;
each of the first body member and the second body member having a generally hollow primary bore, and each of the first body member and second body member being provided with an inlet communicating the respective primary bore with one of the respective gas delivery hose and monitoring hose;
and the primary bore of each of the first body member and second bod? ?mber also having a pair of outlets;
the first body member being provided with two cannula nipples, each of said nipples having a generally hollow secondary bore, and the said secondary bore of each of the cannula nipples of the first body member having an inlet and an outlet, the inlet of the said secondary bore of each of the two cannula nipples of the first body member communicating directly with a respective one of the said two outlets of the primary bore of the first body member;
the second body member being provided with two cannula nipples, each of said nipples having a generally hollow secondary bore, and the said secondary bore of each of the cannula nipples of the second body member having an inlet and an outlet, the inlet of the said secondary bore of each of the two cannula nipples of the second body member communicating directly with a respective one of the said two outlets of the primary bore of the second body member;
the pair of cannula nipples of the first body member and the pair of cannula nipples of the second body member being correspondingly spaced, and the portion of the second body member having the two outlets of its primary bore being located within the primary bore of the first body member, and the cannula nipples of the second body member being located within the secondary bore of the respective cannula nipples of the first body member;
the cannula apparatus providing a cannula nipple outlet for each of a person's nostrils in proximity to one another for both delivering gas to each of the person's nostrils, and monitoring the respiration of the person by monitoring the respiration as to each of the person's nostrils.
the cannula apparatus comprising:
a first body member and a second body member;
each of the first body member and the second body member having a generally hollow primary bore, and each of the first body member and second body member being provided with an inlet communicating the respective primary bore with one of the respective gas delivery hose and monitoring hose;
and the primary bore of each of the first body member and second bod? ?mber also having a pair of outlets;
the first body member being provided with two cannula nipples, each of said nipples having a generally hollow secondary bore, and the said secondary bore of each of the cannula nipples of the first body member having an inlet and an outlet, the inlet of the said secondary bore of each of the two cannula nipples of the first body member communicating directly with a respective one of the said two outlets of the primary bore of the first body member;
the second body member being provided with two cannula nipples, each of said nipples having a generally hollow secondary bore, and the said secondary bore of each of the cannula nipples of the second body member having an inlet and an outlet, the inlet of the said secondary bore of each of the two cannula nipples of the second body member communicating directly with a respective one of the said two outlets of the primary bore of the second body member;
the pair of cannula nipples of the first body member and the pair of cannula nipples of the second body member being correspondingly spaced, and the portion of the second body member having the two outlets of its primary bore being located within the primary bore of the first body member, and the cannula nipples of the second body member being located within the secondary bore of the respective cannula nipples of the first body member;
the cannula apparatus providing a cannula nipple outlet for each of a person's nostrils in proximity to one another for both delivering gas to each of the person's nostrils, and monitoring the respiration of the person by monitoring the respiration as to each of the person's nostrils.
2. The cannula apparatus as set forth in Claim 1, in a combination in which the cannula nipples of the second body member are provided to be sufficiently resiliently flexible that the second body member may be assembled into the primary bore of the first body member, and the cannula nipples of the second body member into the secondary bore of the respective cannula nipples of the first body member,by relatively pushing the second body member into the primary bore of the first body member.
3. The cannula apparatus as set forth in Claim 1, in a combination in which the cross-sectional area of the primary bore of the second body member 18 operatively the same as the difference between the cross-sectional area of the primary bore of the first body member and the cross-sectional area of the outer portion of the second body member, the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas delivery hose or the monitoring hose.
4. The cannula apparatus as set forth in Claim 1, in a combination in which, as to each pair of cannula nipples of the first body member and second body member, the cross-sectional area of the secondary bore of each cannula nipple of the second body member is operatively the same as the difference between the cross-sectional area of the secondary bore of the respective cannula nipple of the first body member and the cross-sectional area of the outer portion of the cannula nipple of the second body member;
the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas delivery hose or the monitoring hose.
the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas delivery hose or the monitoring hose.
5. The cannula apparatus as set forth in Claim 2, in a combination in which the cross-sectional area of the primary bore of the second body member is operatively the same as the difference between the cross-sectional area of the primary bore of the first body member and the cross-sectional area of the outer portion of the second body member, the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas delivery hose or the monitoring hose.
6. The cannula apparatus as set forth in Claim 2, in a combination in which, as to each pair of cannula nipples of the first body member and second body member, the cross-sectional area of the secondary bore of each cannula nipple of the second body member is operatively the same as the difference between the cross-sectional area of the secondary bore of the respective cannula nipple of the first body member and the cross-sectional area of the outer portion of the cannula nipple of the second body member;
the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas delivery hose or the monitoring hose.
the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas delivery hose or the monitoring hose.
7. The cannula apparatus as set forth in Claim 3, in a combination in which, as to each pair of cannula nipples of the first body member and second body member, the cross-sectional area of the secondary bore of each cannula nipple of the second body member is operatively the same as the difference between the cross-sectional area of the secondary bore of the respective cannula nipple of the first body member and the cross-sectional area of the outer portion of the cannula nipple of the second body member;
the operative sameness of cross-sectional areas providing that it ?s a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas delivery hose or the monitoring hose.
the operative sameness of cross-sectional areas providing that it ?s a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas delivery hose or the monitoring hose.
8. Cannula apparatus providing for modified respiration involving gasses "A" and "B" as to a human patient, for use with (a) associated supply equipment for providing for the patient a supply of associated gas "A", and with (b) associated supply equipment for providing for the patient a supply of associated gas "B", the associated supply equipments being provided respectively with a gas "A" delivery hose and a gas "B"
delivery hose, respectively for communication of the gas "A" supply and the gas "B" supply with the cannula apparatus;
the cannula apparatus comprising:
a first body member and a second body member;
each of the first body member and the second body member having a generally hollow primary bore, and each of the first body member and second body member being provided with an inlet communicating the respective primary bore with one of the respective gas "A" delivery hose and gas "B" delivery hose for receiving gas "A" and gas "B" respectively;
and the primary bore of each of the first body member and second body member also having a pair of outlets;
the first body member being provided with two cannula nipples, each of said nipples having a generally hollow secondary bore, and the said secondary bore of each of the cannula nipples of the first body member having an inlet and an outlet, the inlet of the said secondary bore of each of the two cannula nipples of the first body member communicating directly with a respective one of the said two outlets of the primary bore of the first body member;
the second body member being provided with two cannula nipples, each of said nipples having a generally hollow secondary bore, and the said secondary bore of each of the cannula nipples of the second body member having an inlet and an outlet, the inlet of the said secondary bore of each of the two cannula nipples of the second body member communicating directly with a respective one of the said two outlets of the primary bore of the second body member;
the pair of cannula nipples of the first body member and the pair of cannula nipples of the second body member being correspondingly spaced, and the portion of the second body member having the two outlets of its primary bore being located within the primary bore of the first body member, and the cannula nipples of the second body member being located within the secondary bore of the respective cannula nipples of the first body member;
the cannula apparatus providing a cannula nipple outlet for each of a person's nostrils in proximity to one another for delivering both gas "A" and gas "B"
to each of the person's nostrils.
delivery hose, respectively for communication of the gas "A" supply and the gas "B" supply with the cannula apparatus;
the cannula apparatus comprising:
a first body member and a second body member;
each of the first body member and the second body member having a generally hollow primary bore, and each of the first body member and second body member being provided with an inlet communicating the respective primary bore with one of the respective gas "A" delivery hose and gas "B" delivery hose for receiving gas "A" and gas "B" respectively;
and the primary bore of each of the first body member and second body member also having a pair of outlets;
the first body member being provided with two cannula nipples, each of said nipples having a generally hollow secondary bore, and the said secondary bore of each of the cannula nipples of the first body member having an inlet and an outlet, the inlet of the said secondary bore of each of the two cannula nipples of the first body member communicating directly with a respective one of the said two outlets of the primary bore of the first body member;
the second body member being provided with two cannula nipples, each of said nipples having a generally hollow secondary bore, and the said secondary bore of each of the cannula nipples of the second body member having an inlet and an outlet, the inlet of the said secondary bore of each of the two cannula nipples of the second body member communicating directly with a respective one of the said two outlets of the primary bore of the second body member;
the pair of cannula nipples of the first body member and the pair of cannula nipples of the second body member being correspondingly spaced, and the portion of the second body member having the two outlets of its primary bore being located within the primary bore of the first body member, and the cannula nipples of the second body member being located within the secondary bore of the respective cannula nipples of the first body member;
the cannula apparatus providing a cannula nipple outlet for each of a person's nostrils in proximity to one another for delivering both gas "A" and gas "B"
to each of the person's nostrils.
9. The cannula apparatus as set forth in Claim 8, in a combination in which the cannula nipples of the second body member are provided to be sufficiently resiliently flexible that the second body member may be assembled into the primary bore of the first body member, and the cannula nipples of the second body member into the secondary bore of the respective cannula nipples of the first body member,by relatively pushing the second body member into the primary bore of the first body member.
10. The cannula apparatus as set forth in Claim 8, in a combination in which the cross-sectional area of the primary bore of the second body member is operatively the same as the difference between the cross-sectional area of the primary bore of the first body member and the cross-sectional area of the outer portion of the second body member, the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas "A"
delivery hose or the gas "B" delivery hose.
delivery hose or the gas "B" delivery hose.
11. The cannula apparatus as set forth in Claim 8, in a combination in which, as to each pair of cannula nipples of the first body member and second body member, the cross-sectional area of the secondary bore of each cannula nipple of the second body member is operatively the same as the difference between the cross-sectional area of the secondary bore of the respective cannula nipple of the first body member and the cross-sectional area of the outer portion of the cannula nipple of the second body member;
the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas "A" delivery hose or the gas "B" delivery hose.
the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas "A" delivery hose or the gas "B" delivery hose.
12. The cannula apparatus as set forth in Claim 9, in a combination in which the cross-sectional area of the primary bore of the second body member is operatively the same as the difference between the cross-sectional area of the primary bore of the first body member and the cross-sectional area of the outer portion of the second body member, the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas "A"
delivery hose or the gas "B" delivery hose.
delivery hose or the gas "B" delivery hose.
13. The cannula apparatus as set forth in Claim 9, in a combination in which, as to each pair of cannula nipples of the first body member and second body member, the cross-sectional area of the secondary bore of each cannula nipple of the second body member is operatively the same as the difference between the cross-sectional area of the secondary bore of the respective cannula nipple of the first body member and the cross-sectional area of the outer portion of the cannula nipple of the second body member;
the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas "A" delivery hose or the gas "B" delivery hose.
the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas "A" delivery hose or the gas "B" delivery hose.
14. The cannula apparatus as set forth in Claim 10, in a combination in which, as to each pair of cannula nipples of the first body member and second body member, the cross-sectional area of the secondary bore of each cannula nipple of the second body member is operatively the same as the difference between the cross-sectional area of the secondary bore of the respective cannula nipple of the first body member and the cross-sectional area of the outer portion of the cannula nipple of the second body member;
the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas "A" delivery hose or the gas "B" delivery hose.
the operative sameness of cross-sectional areas providing that it is a matter of substantial indifference which of the first body member's inlet or second body member's inlet is operatively connected to the gas "A" delivery hose or the gas "B" delivery hose.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/302,188 US4989599A (en) | 1989-01-26 | 1989-01-26 | Dual lumen cannula |
| CA002072869A CA2072869A1 (en) | 1989-01-26 | 1991-01-29 | Dual lumen cannula |
| EP19910904604 EP0521874A4 (en) | 1989-01-26 | 1991-01-29 | Dual lumen cannula |
| PCT/US1991/000522 WO1992012751A1 (en) | 1989-01-26 | 1991-01-29 | Dual lumen cannula |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/302,188 US4989599A (en) | 1989-01-26 | 1989-01-26 | Dual lumen cannula |
| CA002072869A CA2072869A1 (en) | 1989-01-26 | 1991-01-29 | Dual lumen cannula |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2072869A1 true CA2072869A1 (en) | 1992-07-30 |
Family
ID=25675288
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002072869A Abandoned CA2072869A1 (en) | 1989-01-26 | 1991-01-29 | Dual lumen cannula |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US4989599A (en) |
| EP (1) | EP0521874A4 (en) |
| CA (1) | CA2072869A1 (en) |
| WO (1) | WO1992012751A1 (en) |
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| US9795756B2 (en) | 2012-12-04 | 2017-10-24 | Mallinckrodt Hospital Products IP Limited | Cannula for minimizing dilution of dosing during nitric oxide delivery |
| KR102223425B1 (en) * | 2012-12-04 | 2021-03-08 | 말린크로트 하스피탈 프로덕츠 아이피 리미티드 | Cannula for minimizing dilution of dosing during nitric oxide delivery |
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| WO2018071699A1 (en) * | 2016-10-13 | 2018-04-19 | Vyaire Medical Capital Llc | Nasal cannula systems |
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| US10314999B1 (en) * | 2018-08-23 | 2019-06-11 | Baiping Lei | Nasal breathing apparatus and method for high-flow therapy and non-invasive ventilation |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3172407A (en) * | 1961-09-29 | 1965-03-09 | Baxter Don Inc | Gas administration apparatus |
| US4054133A (en) * | 1976-03-29 | 1977-10-18 | The Bendix Corporation | Control for a demand cannula |
| US4484578A (en) * | 1980-11-26 | 1984-11-27 | Kircaldie, Randall And Mcnab | Respirator apparatus and method |
-
1989
- 1989-01-26 US US07/302,188 patent/US4989599A/en not_active Expired - Lifetime
-
1991
- 1991-01-29 EP EP19910904604 patent/EP0521874A4/en not_active Withdrawn
- 1991-01-29 WO PCT/US1991/000522 patent/WO1992012751A1/en not_active Application Discontinuation
- 1991-01-29 CA CA002072869A patent/CA2072869A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP0521874A1 (en) | 1993-01-13 |
| EP0521874A4 (en) | 1994-07-13 |
| US4989599A (en) | 1991-02-05 |
| WO1992012751A1 (en) | 1992-08-06 |
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Legal Events
| Date | Code | Title | Description |
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| FZDE | Dead |